Stuart Hutter
Advisor: Tilahun Adera, MPH, PhD
Preceptor: Robert
Suruki, ScD
Introduction: Asthma is a common debilitating disease
of the airways that afflicts an estimated 300 million worldwide, causing
reduction in physical activity, lost school/work days, and even death. There
are many known and suspected risk factors of asthma; however, there is
much controversy over prior and current cigarette smoking. Approximately
25% of the United States population currently smokes, with a quarter of
these being asthma patients. Another 22 to 43 percent of asthmatics
are ex-smokers.
Objectives: (1) To estimate the prevalence for lifetime asthma
in the adult US population; (2) to determine prevalence odds ratios (POR) of
lifetime asthma based on questionnaire (smoking status, tobacco consumption)
after adjustment of potential confounding variables; (3) to determine POR of
lifetime asthma based on laboratory values (serum cotinine); and (4) to assess
the validity of self-reported measures (smoking status and tobacco consumption)
using serum cotinine as the gold standard.
Methods: The National Health and Nutrition Examination Survey (NHANES) 1999-2002 is a proportional cross-sectional sample that uses weights to be representative. Crude odds ratios were obtained through univariate analysis; multiple logistic regression analysis was used to obtain adjusted odds ratios of asthma. Interactions for age, gender, and race/ethnicity were explored. Validity measures included sensitivity and specificity tests for self-reported smoking and non-parametric correlation of tobacco consumption with serum cotinine levels.
Results: The overall prevalence of lifetime asthma among
n=10,252 adults was 11.56% (95%CI 10.45-12.66). Analyses were stratified
by race/ethnicity due to significant interaction. After adjusting
for age, gender, body mass index, and family history of asthma, ex-smoking
non-Hispanic Whites, non-Hispanic Blacks, and other races had odds ratios
of 1.57 (95%CI 1.26-1.97), 1.52 (95%CI 1.01-2.27), and 1.97 (95%CI 1.01-3.83),
respectively, relative to never smokers within their respective race/ethnic
groups. Sample persons with a family history of asthma and increasing
body mass index were significant predictors for lifetime asthma among all
race/ethnic groups. Based on laboratory values, non-Hispanic White
respondents with serum cotinine levels of 0.011 to <15ng/ml and ≥15ng/ml
were 61% (9-138%) and 38% (4-83%), respectively, more likely to have lifetime
asthma relative to non-Hispanic Whites with undetectable levels. No
dose-dependent relationship is evident. Self-reported smoking showed
92% sensitivity and 94% specificity with a positive predictive value of
88%. The overall smoker misclassification rate was 2.45%. Daily
tobacco consumption was significantly correlated with serum cotinine in
the total population (r=0.532, p < 0.0001).
Discussion: Self-reported smoking and tobacco consumption
are valid measures of tobacco use. The present study found no significant
relationship between current smoking and lifetime asthma. Despite the limited
findings, asthmatic smokers make up a distinct, difficult-to-treat subgroup
for which future treatment research should address.